任职要求/岗位职责
请同时发送中英文双语的简历！附发表的文章或科研资料介绍更好！
简历请同时转发至szjiangqun@163.com；uschumacher@hotmail.com；ursula.schumacher@suzhouresearch.com.cn和hanzi2.14@163.com
Serve as a scientist for assigned preclinical research studies of basic to moderate complexity, to include study management, interpretation and reporting of study data, and assuring the regulatory compliance of these projects.
•； ESSENTIAL DUTIES AND RESPONSIBILITIES:
•； With minimal guidance, serve as a as a study director (SD), project scientist (PS) and/or principal investigator (PI) in the direction and ution of assigned studies in compliance with GLP regulations as they apply to the conduct of nonclinical research.
•； Participate in and coordinate all phases of the study planning process with appropriate departments.
•； Generate high-quality project plans, protocols, amendments, and reports appropriate for assigned studies.
•； Review, interpret, integrate, and present data on assigned studies, using the assistance of senior scientific staff as appropriate.
•； Function as contact for the planning and ution of sponsor interaction related to assigned studies, including proposal management and study scheduling, conduct and reporting.
•； Provide technical and scientific guidance to the research staff.
•； Attend scientific meetings, conferences and training courses to enhance job and professional skills.
•； Perform all other related duties as assigned.
Education/Qualifications/Experience:
•； PhD or DVM preferred.
•； Minimum of 1 to 5 years related experience in the contract research, academic, or pharmaceutical industry.
•； An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Other: Understanding of the scientific basis of “General Toxicology” and the Testing Guidelines (e.g. ICH M3, S3A, S3B, S4, S9, S6, as well as OECD etc.) of study types assigned, as well as Testing Facility SOPs and the Good Laboratory Practices (GLPs), as appropriate. Effective written and verbal communication skills. Ability to handle multiple projects, prioritize work and meet deadlines. Proficiency in the use of computerized Preclinical Data Acquisition and Biostatistical Software with standard laboratory calculations is a plus.
企业介绍
苏州西山中科药物研究开发有限公司（苏州药物安全性评价研究中心）是一家国有企业，主要从事药物临床前研究和开发和化学品的安全测试。公司目前地处苏州太湖国家旅游度假区，青山绿水，风光璇妮，景色宜人。今年上半年公司将整体搬迁至吴中经济开发区（吴中科技园），新大楼建筑面积20600平方米。苏州西山中科药物研究开发有限公司拥有“药物药效学评价研究中心”、“药物代谢动力学研究中心”、“药物安全性评价研究中心（GLP）”和“化学品安全测试中心”。形成了一个完整的实验动物相关产业研究服务平台，旨在为国内外客户提供高水平的新药非临床药代动力学、药效学、安全性评价服务，以及符合欧盟标准的化学品安全评价服务。公司的理念：以药物临床前研究质量管理规范（GLP）保证药物研究和开发的质量。公司的文化：和谐、务实、创新、进取。公司的战略目标：在3—5年内成为亚洲一流的药物临床前研究机构和化学品安全测试中心。公司运作机制为董事会领导下的总经理负责制。公司技术力量雄厚，拥有6位博士（其中2位为留美海归博士、一位德籍专家），10位硕士以及一批具有娴熟实验操作技术的科研人员。公司具有大动物房（中央空调），能开展犬和猴的实验研究；具有病理、临床检验、毒理研究实验室；具有质量保证部门、动物伦理委员会、样品和档案管理、信息管理等行政部门；拥有先进的仪器设备，其中大部分为进口品牌机。公司通过自己撰写的标准操作规程（SOPs）规范实验研究，以保证实验结果的科学、可靠、可信。公司近3年完成和正在研究的国家科技部、江苏省和苏州市的科研项目9项；完成和正在进行的国内研究项目150项，其中部分为美国和加拿大委托的研究项目。公司具有完整的管理规章制度，具有合理的薪酬制度和激励机制，为每一个公司员工提供良好的工作氛围和发展机会。公司竭诚欢迎有至于从事药物研究和开发及化学品安全测试的科技人员加盟我们的团队！
SUZHOU XISHAN ZHONGKE Drug R&D Co., Ltd is subdivided into 4 research centers: Pharmacodynamic Research Center, Pharmacokinetic Research Center, Drug Safety Evaluation and Research Center (SFDA-approved GLP Lab) and Chemical Safety Testing Center (OECD Guidelines). SUZHOU XISHAN ZHONGKE specializes in contract research and regulatory compliance for the pharmaceutical, agrichemical and chemical industries. Since 10 years, SUZHOU XISHAN ZHONGKE has obtained a reputation for quality in preclinical toxicology, drug research and recently Ecotoxicology. SUZHOU XISHAN ZHONGKE serves a global client base as well as domestic private and public organizations.
SUZHOU XISHAN ZHONGKE is a team of innovative professionals providing high-quality, timely, value-added services to our clients. Our success is achieved through honesty in thought, word and action toward our clients, fellow employees, communities and suppliers, characterized by ethical conduct and sincerity of purpose.
SUZHOU XISHAN ZHONGKE offers competitive salaries and an attractive benefit plan.
联系人：蒋群
传真：0512-66370161
联系地址：苏州市吴中区金庭镇居山湾
单位网站：www.suzhouresearch.com.cn
